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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of Proteus Syndrome and Related Congenital DisordersAbnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cowden disease, Limb Deformities, Congenital, Musculoskeletal Abnormalities, Neoplasms, Multiple Primary, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Proteus syndrome, bone disorder, hamartoma, hereditary endocrine growth disease, musculoskeletal system disorder, neoplasmRecruitingNot stated2026-09-22NCT00001403
MK-7075 (Miransertib) in Proteus SyndromeAbnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cowden disease, Limb Deformities, Congenital, Musculoskeletal Abnormalities, Neoplasms, Multiple Primary, Proteus syndrome, bone disorder, hamartoma, musculoskeletal system disorder, neoplasmActive, not recruitingPhase 22026-07-17NCT04316546